|
131
|
|
|
NECAP endocytosis associated 1 |
DEE21, EIEE21 |
|
|
132
|
|
|
NMDA receptor synaptonuclear signaling and neuronal migration factor |
HH9, NELF |
Carcinoma, Hypogonadotropic hypogonadism, Hypopituitarism, Growth hormone deficiency, Kallmann syndrome, Liver cirrhosis, Male infertility single gene azoospermia, Panhypopituitarism, Pituitary dwarfism, Pituitary short stature, Pituitary stalk interruption syndrome, Sheehan syndrome |
|
133
|
|
|
NOC2 like nucleolar associated transcriptional repressor |
NET15, NET7, NIR, PPP1R112 |
|
|
134
|
|
|
Nephrocystin 4 |
POC10, SLSN4 |
Alzheimer disease, Bardet-biedl syndrome, Behcet disease, Congenital anomalies of the kidney and urinary tract, Cholelithiasis, Kidney disease, Congenital heart disease, Joubert syndrome, Juvenile idiopathic arthritis, Nephronophthisis, Leber congenital amaurosis, Nephronophthisis, familial juvenile, Optic atrophy, Retinitis pigmentosa, Senior-loken syndrome |
|
135
|
|
|
Nuclear protein 1, transcriptional regulator |
COM1, P8 |
Crohn disease, Heart failure, Inflammatory bowel disease, Leprosy, Lipidoses, Lipoidosis, Liver cirrhosis, Pancreatitis, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Ulcerative colitis |
|
136
|
|
|
Neuronal PAS domain protein 4 |
Le-PAS, NXF, PASD10, bHLHe79 |
|
|
137
|
|
|
Neurobeachin |
BCL8B, LYST2, NEDEGE |
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Nonsyndromic intellectual disability, Cerebellar, ocular, craniofacial, and genital syndrome, Color vision deficiency, Neurodevelopmental disorder, Developmental disability, Diverticulitis, Epilepsy, Human immunodeficiency virus infection, Intellectual developmental disorder, Interstitial lung disease, Liver cirrhosis, Migraine, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Obstructive sleep apnea syndrome, Peripheral arterial disease, Substance abuse, Systemic sclerosis, Urinary bladder cancerView all (7 more) |
|
138
|
|
|
Neuroplastin |
GP55, GP65, SDFR1, SDR1, np55, np65 |
|
|
139
|
|
|
Nephrocystin 3 |
CFAP31, MKS7, NPH3, RHPD, RHPD1, SLSN3 |
Anhydramnios, Hemolytic uremic syndrome, Polycystic kidney disease, Bardet-biedl syndrome, Aplasia of the vermis, Hypertension, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Meckel syndrome, Meckel-gruber syndrome, Nephronophthisis, Optic atrophy, Retinitis pigmentosa, Senior-loken syndrome |
|
140
|
|
|
NADPH oxidase 1 |
GP91-2, MOX1, NOH-1, NOH-1L, NOH1 |
|
